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1203271

CC(C)CN(C(=O)CCl)c1nc(-c2ccccc2Cl)c(-c2ccc(Cl)cc2)cc1C#N
Reaction #42114
2-chloro-N-(6-(2-chlorophenyl)-5-(4-chlorophenyl)-3-cyanopyridin-2-yl)-N-isobutylacetamide
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc2c(nc1N)CCN(Cc1ccccc1)C2
Reaction #49975
2-amino-6-benzyl-5,6,7,8-tetrahydro-1,6-naphthyridine-3-carbonitrile
Выход 49.5%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc2c(nc1N)CCN(Cc1ccccc1)C2
Reaction #49978
2-amino-6-benzyl-5,6,7,8-tetrahydro-1,6-naphthyridine-3-carbonitrile
Выход 49.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C#N)c(C=O)nc1N1CCCCC1
Reaction #56038
5-Cyano-6-formyl-2-piperidinyl-3-pyridine-carboxylic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=C1NC(N2CCCCC2)=C(C(=O)OCC)C(NN)=C1C#N
Reaction #56039
5-Cyano-6-methylidene-hydrazino-2-piperidinyl-3-pyridine-carboxylic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(-c2ccccc2)cc(N2CCOCC2)nc1Cl
Reaction #56159
2-chloro-6-morpholino-4-phenyl-3-cyano-pyridine
Выход 86.1%DOI: 10.6084/m9.figshare.5104873.v1
Nc1n[nH]c2nc(N3CCOCC3)cc(-c3ccccc3)c12
Reaction #56160
3-amino-6-morpholino-4-phenyl-1H-pyrazolo[3,4-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(NCCNc2ncc(-c3ncc[nH]3)c(-c3ccc(F)cc3C(F)(F)F)n2)nc1
Reaction #60168
6-{[2-({4-[4-fluoro-2-(trifluoromethyl)phenyl]-5-imidazol-2-ylpyrimidin-2-yl}amino)ethyl]amino}pyridine-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(NCCNc2ncc(-c3ncc[nH]3)c(-c3ccc(C(F)(F)F)cc3F)n2)nc1
Reaction #60175
6-{[2-({4-[2-fluoro-4-(trifluoromethyl)phenyl]-5-imidazol-2-ylpyrimidin-2-yl}amino)ethyl]amino}pyridine-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)ccc1-c1nc(NCCNc2ccc(C#N)cn2)ncc1-c1ncc[nH]1
Reaction #60179
6-[(2-{[4-(4-chloro-2-methoxyphenyl)-5-imidazol-2-ylpyrimidin-2-yl]amino}-ethyl)amino]pyridine-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ccc(C#N)cn2)c1
Reaction #89259
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)N1C2CCC1CC(NC(=O)N1CC[C@@H](Nc3ccc(C#N)cn3)C1)C2
Reaction #159328
title compound
Выход 58.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Nc1nc(Nc2cc(C3CC3)[nH]n2)c(F)cc1C#N)c1ccc(F)cc1
Reaction #163085
title compound
Выход 28.9%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)C3CSCCN43)CC2)nc1
Reaction #173448
DOI: 10.1039/C8SC04228D
N#Cc1c(N)nc(SCc2csc(-c3ccc(Cl)cc3)n2)c(C#N)c1C1CCC(O)CC1
Reaction #178547
DOI: 10.1039/C8SC04228D
CC1CN(c2ccc3c(c2)c(NCc2ccccc2)c(C#N)c(N)[n+]3N)CC(C)O1
Reaction #186239
DOI: 10.1039/C8SC04228D
N#Cc1c(N)nc(OCc2coc(-c3ccc(Cl)cc3)n2)c(C#N)c1-c1ccc(OCCO)cc1
Reaction #194791
DOI: 10.1039/C8SC04228D
N#Cc1cnc2ccc([N+](=O)[O-])cc2c1Nc1ccc(Br)c(Br)c1
Reaction #200614
DOI: 10.1039/C8SC04228D
N#Cc1ccc(NCCNc2nc(-c3ccc(C(F)(F)F)cc3)cc3ncnn23)nc1
Reaction #204189
DOI: 10.1039/C8SC04228D
COc1cc(Nc2c(C#N)cnc3cc(-c4ccc(CN5CCCC5C(N)=O)cc4)ccc23)c(Cl)cc1Cl
Reaction #204606
DOI: 10.1039/C8SC04228D
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